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Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
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Junior Member
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This has been a long holiday weekend.... I don't yet have a diagnosis but here's my symptom history:
fluctuating ptosis (droopy eye) -- 41+ years (since at least age 3) difficulty breathing /severe shortness of breath when exercising -- 19-20+ years racing heart, extremely elevated heart rate (200+bpm) when exercising -- 19-20+ years (Note: was diagnosed with ‘Exercise-Induced Bronchospasms not associated with asthma’ Aug 2011) memory loss -- many years muscle spasms/tightness in leg that wouldn’t release or relax (right now seems fine) -- 3-4 years severe lower back pain -- 3-4 years sleep apnea (suspected) -- 1 year or less increased sensitivity to noise -- 3-4 months? fasciculations on monitor during cervical decompression therapy (actuator tension works to create defensive contractions 30 milliseconds ahead of the body. Whereas a typical bodily response is for the line to become steady with relaxation, mine became extremely erratic the more I relaxed -- June-July 2012) pitting edema in legs & face -- first noticed after working out 2 mths ago or so mid-Oct 2012, I started using Whole Body Vibration Machine to try & reduce pitting edema. Machine is also known to ‘tone muscles’. I believe it triggered excess muscular fatigue which led to the sudden addition of multiple symptoms: bruxism (teeth grinding) - broke off a crown, loosened a tooth & 2 other crowns (have started using mouthguard) -- Oct 2012 choking -- most recently during last 2 weeks imbalance -- during last 2 weeks urinary incontinence round the clock -- during last 2 weeks worsening of shortness of breath -- during last 2 weeks hearing worsened -- noticed it during last 2 weeks blurry vision -- noticed only 1-2 times during last 2 weeks aspirated saliva & liquids multiple times -- during last 2 weeks, 8 incidences regurgitating into oral cavity -- last 2 weeks arm, shoulder & hand weakness & pain -- 2 weeks for arm weakness, ache since Nov 24 leg weakness & muscles burning sensation -- noticed 1 week ago substernal chest pain with chest pain flaring up when lying on left side -- since Nov 21 or 22 excess saliva & drooling -- since Nov 21 or 22 pain in back of neck -- since Nov 23 My mom had four (known to me) Autoimmune Diseases, I have three known with MG being the 4th if it is diagnosed. And I know those with vitiligo & Hashimoto's and severe B12 deficiency are inclined toward myasthenia when collecting add'l Autoimmune diseases via what I've read about Type 3 MAS or PAS 3C. Long intro. Anyway, my point.... I went to the E.R. Black Friday, concerned about myasthenic crisis (because of chest pain & 7 (at that count) incidences of aspirating fluid in 2 weeks). Internet & BCBS nurse said I should go so I did. The *edit* of an E.R. doctor accused me of being a hypochondriac & said I've spent too much time online. *edit* ever. Anyway, I left after he refused to do any MG-detecting tests other than acetylcholine AB which takes a couple business days for results. Meanwhile, I was sent home. My concern: despite resting pretty much round-the-clock, the chest pain continues & becomes near constant if I lie on my left side. The pain also shifts from the center of my chest more to the left side. Should I be concerned? Do I need to go to the E.R. again despite the likely repeat poor reception & financial expense? Am I being stupid to think I can wait until tomorrow to finally speak with my doctor & other health professionals who were absent during this frustratingly long holiday weekend? Last edited by Chemar; 11-25-2012 at 08:47 PM. Reason: Language Guidelines |
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